Dynamics of membrane adhesion : the role of polyethylene glycol spacers, ligand-receptor bond strength, and rupture pathway

Biological adhesion typically occurs through discrete cross bridges between complementary molecules on adjacent membranes. Here we report quantitative measurements of the binding distance between a lipid membrane functionalized with ligands on flexible polymer tether chains and a second membrane bea...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 24(2008), 4 vom: 19. Feb., Seite 1225-31
1. Verfasser: Wong, Joyce Y (VerfasserIn)
Weitere Verfasser: Kuhl, Tonya L
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2008
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. Ligands Lipid Bilayers Phosphatidylethanolamines 1,2-distearoylphosphatidylethanolamine 1G4B5265CQ Polyethylene Glycols 3WJQ0SDW1A mehr... 1,2-dilauroylphosphatidylethanolamine 53695-34-4 Biotin 6SO6U10H04 Streptavidin 9013-20-1
Beschreibung
Zusammenfassung:Biological adhesion typically occurs through discrete cross bridges between complementary molecules on adjacent membranes. Here we report quantitative measurements of the binding distance between a lipid membrane functionalized with ligands on flexible polymer tether chains and a second membrane bearing complementary receptors using the surface force apparatus technique. The binding distance is shown to increase as a function of polymer tether length. Upon separation, adhesive failure occurs not at the strong ligand-receptor bond but primarily through the mechanical pullout of cross-bridging polymer tethers from the membrane. We summarize these measurements of complementary membrane adhesion dynamics using an energy-state diagram that encompasses the energetics of the polymer tether, ligand-receptor bond strength, and number of cross bridges formed
Beschreibung:Date Completed 07.05.2008
Date Revised 01.12.2018
published: Print-Electronic
Citation Status MEDLINE
ISSN:1520-5827
DOI:10.1021/la702357a